Canonical Allele Identifier: CA356792388

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42965051C>G (hg19) ; chr4:g.42963034C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42963034C>G , CM000666.2:g.42963034C>G	GRCh38
NC_000004.11:g.42965051C>G , CM000666.1:g.42965051C>G	GRCh37
NC_000004.10:g.42659808C>G	NCBI36
NG_027718.1:g.74769C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.527C>G MANE Select	ENSP00000382670.2:p.Ala176Gly
ENST00000399770.2:c.527C>G	ENSP00000382670.2:p.Ala176Gly
NM_001080476.2:c.527C>G	NP_001073945.1:p.Ala176Gly
XM_011513691.1:c.164C>G	XP_011511993.1:p.Ala55Gly
NM_001080476.3:c.527C>G MANE Select	NP_001073945.1:p.Ala176Gly